10 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
POLYAXIAL SCREW DRIVER
FDA Adverse Event
Malfunction
·SEASPINE, INC.·Product code HXX·October 25, 2013
POLYAXIAL SCREW DRIVER
FDA Adverse Event
Malfunction
·SEASPINE, INC.·Product code HXX·January 18, 2014
POLYAXIAL SCREW DRIVER
FDA Adverse Event
Malfunction
·SEASPINE, INC.·Product code HXX·October 25, 2013
PREMIER ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWQ·August 12, 2011
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 7, 2015
HEMOPRO2 EXTENSION CABLE
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC.·Product code GEI·May 13, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·July 10, 2015
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·January 11, 2013